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TSPY1 (testis specific protein Y-linked 1)
Gene
Gene Gene ontology Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7258
Gene nameGene Name - the full gene name approved by the HGNC.
Testis specific protein Y-linked 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
TSPY1
SynonymsGene synonyms aliases
CT78, DYS14, TSPY, pJA923
ChromosomeChromosome number
Y
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Yp11.2
SummarySummary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is found only in testicular tissue and may be involved in spermatogenesis. Many functional paralogs and pseudogenes of this gene are present in a cluster in humans, but only a single, nonfunctional orthologous gene is foun
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
Gene Gene ontology Other IDs Associated diseases
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin IBA 21873635
GO:0003674 Function Molecular_function ND
GO:0003682 Function Chromatin binding IBA 21873635
GO:0005515 Function Protein binding IPI 18649364
GO:0005575 Component Cellular_component ND
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Gene ontology Other IDs Associated diseases
MIM
HGNC
e!Ensembl
Interactions View interactions
Associated diseases
Gene Gene ontology Other IDs Associated diseases
Causal
Disease name Disease term dbSNP ID References
Cryptorchidism Cryptorchidism rs121912555, rs104894697, rs104894698, rs398122886
Non-obstructive azoospermia Non-obstructive azoospermia rs587777872, rs879253743, rs1600840291, rs1600877766, rs753462162, rs1588618614, rs1602684496, rs377712900
Oligospermia Oligospermia rs1602125411, rs2047796277, rs377712900
Unknown
Disease name Disease term dbSNP ID References
Partial chromosome y deletion Partial chromosome Y deletion

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